OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Molecular functions of MCM8 and MCM9 and their associated pathologies
Noah C. Helderman, Diantha Terlouw, Laia Bonjoch, et al.
iScience (2023) Vol. 26, Iss. 6, pp. 106737-106737
Open Access | Times Cited: 11

Showing 11 citing articles:

Novel Copy Number Deletion Involving NUS1 Associated With Epilepsy, Tremor, and Intellectual Disability
Jing Y. Hsu, Daniah H. Ibrahim, Riza Ali, et al.
Clinical Case Reports (2025) Vol. 13, Iss. 1
Open Access | Times Cited: 1

Primary ovarian insufficiency: update on clinical and genetic findings
Silvia Federici, Raffaella Rossetti, Silvia Moleri, et al.
Frontiers in Endocrinology (2024) Vol. 15
Open Access | Times Cited: 5

Unwinding Helicase MCM Functionality for Diagnosis and Therapeutics of Replication Abnormalities Associated with Cancer: A Review
Arathi Radhakrishnan, Ritwik Gangopadhyay, Chandresh Sharma, et al.
Molecular Diagnosis & Therapy (2024) Vol. 28, Iss. 3, pp. 249-264
Closed Access | Times Cited: 4

Novel Copy Number Deletion involving NUS1 associated with Epilepsy, Tremor, and Intellectual Disability
Gholson J. Lyon, Jing Y. Hsu, Daniah H. Ibrahim, et al.
Authorea (Authorea) (2024)
Open Access | Times Cited: 1

Cell cycle arrest combined with CDK1 inhibition suppresses genome-wide mutations by activating alternative DNA repair genes during genome editing
Nozomi Fukuda, Keisuke Soga, Chie Taguchi, et al.
Journal of Biological Chemistry (2024) Vol. 300, Iss. 9, pp. 107695-107695
Open Access | Times Cited: 1

Understanding the novelMCM8gene mutation: primary ovarian insufficiency and uterine hypoplasia in siblings
R.K. Mishra, Naresh Kumar, Arun Bargali, et al.
BMJ Case Reports (2024) Vol. 17, Iss. 7, pp. e259433-e259433
Closed Access

HROB Is Implicated in DNA Replication
J. Nathan Kutz, Hannes Schmietendorf, Shibley Rahman, et al.
Genes (2024) Vol. 15, Iss. 12, pp. 1587-1587
Open Access

Pharmacogenomic studies of fertility outcomes in pediatric cancer survivors – A systematic review
Tayla Stenta, Michael Assis, Katie L. Ayers, et al.
Clinical and Translational Science (2024) Vol. 17, Iss. 6
Open Access

Clinical syndromes linked to biallelic germline variants inMCM8andMCM9
Noah C. Helderman, Ting Yang, Claire Palles, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access

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